A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3280n100



Internal ID22789367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72776654..72817519hg38UCSC Ensembl
chr17:70772793..70813658hg19UCSC Ensembl
chr17:68284388..68325253hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3840866
hg1940866
hg1840866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057711, nsv1058434, nsv1061183
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3280n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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